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A boy and his father with hereditary hypotrichosis simplex were treated for hair loss, but the treatment result is unknown.

Mutations in the P2RY5 gene cause hereditary woolly hair.

Tranexamic acid effectively reduced swelling episodes in a girl with a rare form of hereditary angioneurotic edema.

PCOS is a hereditary disorder that can lead to diabetes and heart disease if not treated early.

Caffeine may help hair growth in hereditary hair loss.

New treatments are being explored to slow or reverse hereditary hair loss.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

A disease causing skin issues in young adult German short-haired pointers is hereditary, with most affected dogs not responding to treatment.

Eyebrow reconstruction using hair follicle grafts was successful in a man with a benign hereditary disorder affecting his eyebrows.

The young woman has a benign, hereditary skin condition with no signs of a more serious syndrome.

Three related Persian cats have a rare, likely hereditary skin condition causing hair loss and poor coat quality, with limited treatment options.

HDMHG0401-10 treatment significantly improved hair count and was better than a placebo in reducing hair loss in men with hereditary hair loss, with no major side effects.

Some horses lose hair without inflammation or itching due to various conditions, and while mainly a cosmetic issue, diagnosis requires examination and biopsies, and breeding is not advised if it's hereditary.

Early surgery reduces seizure risk in drug-resistant epilepsy; testosterone to DHT conversion doesn't affect muscle anabolism; veterans with PTSD likely to have riskier opioid use; bevacizumab helps in hereditary bleeding disorder.

The vitamin D receptor is crucial for bone health and affects various body systems, with mutations potentially leading to disease.

Two rare genetic diseases cause severe rickets in children due to defects in vitamin D metabolism.

Eating high glycemic foods and drinking milk may worsen acne by increasing insulin and IGF-1 levels.

Two new proteins, hKAP1.6 and hKAP1.7, are found in the hair follicle cortex.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

A vitamin D receptor mutation causes rickets and affects immune responses.

The conclusion suggests a new way to classify bradykinin-mediated angio-oedema based on different causes and its possible link with urticaria, which could improve diagnosis and treatment.

The document emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.

Hair restoration in children, tailored to their specific needs, can yield good aesthetic results with minimal complications.

The document concludes that hair loss in cats is caused by various factors, including allergies, mites, infections, and hormonal issues, with treatments varying accordingly.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

The R343H mutation in the VDR gene causes vitamin D-resistant rickets with alopecia by impairing specific gene activity.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

Many women's hair loss is due to health issues, medication, nutrition, or stress.